Canonical Allele Identifier: CA377160390
Gene: CDH23 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71740847C>A , CM000672.2:g.71740847C>A GRCh38
NC_000010.10:g.73500604C>A , CM000672.1:g.73500604C>A GRCh37
NC_000010.9:g.73170610C>A NCBI36
NG_008835.1:g.348901C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000224721.12:c.4514C>A MANE Select ENSP00000224721.9:p.Pro1505His
ENST00000224721.10:c.4529C>A ENSP00000224721.8:p.Pro1510His
ENST00000398792.3:n.1203C>A
ENST00000622827.4:c.4514C>A ENSP00000483211.1:p.Pro1505His
NM_022124.5:c.4514C>A NP_071407.4:p.Pro1505His
XM_006717940.2:c.4709C>A XP_006718003.1:p.Pro1570His
XM_006717942.2:c.4643C>A XP_006718005.1:p.Pro1548His
XM_011540039.1:c.4706C>A XP_011538341.1:p.Pro1569His
XM_011540040.1:c.4703C>A XP_011538342.1:p.Pro1568His
XM_011540041.1:c.4649C>A XP_011538343.1:p.Pro1550His
XM_011540042.1:c.4709C>A XP_011538344.1:p.Pro1570His
XM_011540043.1:c.4709C>A XP_011538345.1:p.Pro1570His
XM_011540044.1:c.4574C>A XP_011538346.1:p.Pro1525His
XM_011540045.1:c.4709C>A XP_011538347.1:p.Pro1570His
XM_011540046.1:c.4169C>A XP_011538348.1:p.Pro1390His
XM_011540047.1:c.3527C>A XP_011538349.1:p.Pro1176His
XM_011540048.1:c.4709C>A XP_011538350.1:p.Pro1570His
XM_011540049.1:c.4709C>A XP_011538351.1:p.Pro1570His
XM_011540050.1:c.4709C>A XP_011538352.1:p.Pro1570His
XM_011540051.1:c.4709C>A XP_011538353.1:p.Pro1570His
XM_011540052.1:c.1037C>A XP_011538354.1:p.Pro346His
XM_011540053.1:c.4709C>A XP_011538355.1:p.Pro1570His
XR_945796.1:n.4952C>A
NM_022124.6:c.4514C>A MANE Select NP_071407.4:p.Pro1505His